Job offers for Drug Safety Associate jobs in the United Kingdom

Top Job | Fulltime |

18 month contract - Top Pharma - Maidenhead - Drug Safety Associate* My client a leading multinational pharmaceutical, medical devices and consumer packaged goods manufacturing company is currently looking for a Drug Safety Associate to join their Safety team. Your new role As the Drug Safety

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Drug Safety Associate (Operations), UK Affiliate is to • Manage UK and Republic of Ireland (ROI) adverse event and device reports in accordance with local and global standard operating procedures (SOPs) and regulations. • Collaborate with internal and external customers. • Provide appropriate

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13/04/2018 | Fulltime |

Drug Safety Associate (Operations), UK Affiliate is to • Manage UK and Republic of Ireland (ROI) adverse event and device reports in accordance with local and global standard operating procedures (SOPs) and regulations. • Collaborate with internal and external customers. click apply for full job

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24/04/2018 | Fulltime

Launches and the Regulatory approval of promotional materials Working with country teams to establish and implement Regulatory Strategies Supporting relevant teams to ensure compliance within Drug Safety Working closely with commercial teams Interaction with relevant health authorities such as the MHRA to

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24/04/2018 | Fulltime

Overview The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable

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Ingredients, drug delivery and formulation to regulatory affairs, safety, bioavailability, mergers and acquisitions. Key Objectives Drive the editorial development of the platforms and associated brand extensions by · Championing a clear and differentiated editorial road-map for the titles, driven by core

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24/04/2018 | Fulltime

Worth of vouchers. JCW Life Sciences JCW is a recruitment company operating in the Life Sciences space, with specialist consultants working within the technical and regulatory areas. This includes the following markets; - Pharmacovigilance/Drug Safety - Regulatory Affairs - Quality Assurance - Quality

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23/04/2018 | Fulltime |

Studies supported by the CDR are often, but not exclusively, comparative safety and efficacy (phase 3) trials that are high-enrolling and require robust data capture. - Review tasks include both point-to-point data checks and interpretive analysis that requires that the CDR be knowledgeable about the

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Top Job | Fulltime |

Drug Safety Associate I activities include (but are not limited to) i. Receipt, validation, and analysis of source document(s) and completion of data entry in LSS as appropriate. ii. Perform assessment of expectedness of adverse events against the Reference Safety Information, as required. iii

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For a Medical Information Associate. You will communicate with Swedish healthcare professionals, responding to a variety of enquiries about the company`s drug products. This is a rare opportunity which will be an excellent step forward in your career. The ideal candidate will be a Swedish national

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23/04/2018 | Fulltime |

Delivery - Ensure contractual obligations are met - Manage budgets and revenue streams associated with works - Ensure billing is undertake to recover costs - Manage the compensation and variation process for new works - Seek new opportunities with clients - Carry out operational SAP duties at 11kV (33kV

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23/04/2018 | Fulltime |

Regulatory Operations Associate job opportunity at their offices in Cambridge. The company has a growing pipeline of investigational drugs and approximately 5,000 employees in offices across four continents. Job Responsibilities - Responsible for preparing regulatory submissions which require

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PPD is looking to recruit a Pharmacovigilance (PVG) Safety Specialist (SS) to be based at our Cambridge office. Working within the PVG department, the PVG SS will submit all submissions with regulatory timelines, to appropriate quality standards and following PPD procedures. The PVG SS will also

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For a Medical Information Associate. You will communicate with Swedish healthcare professionals, responding to a variety of enquiries about the company’s drug products. This is a rare opportunity which will be an excellent step forward in your career. The ideal candidate will be a Swedish national

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